Cargando…

When Hypereosinophilia Leads to Stroke

AFIP1L1-PDGFRA fusion can only be confirmed through molecular and cytogenetic investigations causing a delay in the diagnosis. However, patients with this mutation need urgent treatment because they present hypereosinophilia which may be associated with short-term tissue damage. Thromboembolism is a...

Descripción completa

Detalles Bibliográficos
Autores principales: Chalayer, Emilie, Pelissier, Aude, Tardy, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SMC Media Srl 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346789/
https://www.ncbi.nlm.nih.gov/pubmed/30755950
http://dx.doi.org/10.12890/2017_000614
Descripción
Sumario:AFIP1L1-PDGFRA fusion can only be confirmed through molecular and cytogenetic investigations causing a delay in the diagnosis. However, patients with this mutation need urgent treatment because they present hypereosinophilia which may be associated with short-term tissue damage. Thromboembolism is a known cause of death in hypereosinophilic syndrome. A case of Loeffler endocarditis due to FIP1L1-PDGFRA-associated chronic eosinophilic leukemia presenting hemiparesis with fever, which also mislead the initial diagnosis, is reported. LEARNING POINTS: FIP1L1-PDGFRA fusion occurs in 10% of patients with idiopathic hypereosinophilia. Thromboembolism is a known cause of death in hypereosinophilia. The prognosis of FIP1L1-PDGFRA-associated chronic eosinophilic leukemia has been profoundly changed by imatinib treatment.